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Updated: Aug 8, 2026

Isolation of Precursor B-cell Subsets from Umbilical Cord Blood
Published on: April 16, 2013
B8.7 antigen is present on B-cell precursor acute lymphocytic leukemia. Correlation with the low molecular weight
C Leprince1, N Blumenfeld, G Flandrin
1Inserm U 131, Clamari, France.
Insights
B8.7 antigen expression correlates with low molecular weight B-Cell growth factor (LMW BCGF) responsiveness in early B-cell differentiation. This suggests B8.7 plays a role in the LMW BCGF pathway in B-cell precursor acute lymphoblastic leukemias (ALL).
Area of Science:
- Immunology
- Hematology
- Cell Biology
Background:
- B-cell differentiation involves complex signaling pathways.
- Acute lymphoblastic leukemia (ALL) originates from immature B-cells.
- Understanding early B-cell development is crucial for leukemia research.
Purpose of the Study:
- To investigate B8.7 antigen expression in human B-cell precursor ALL.
- To determine the functional role of B8.7 antigen in the low molecular weight B-Cell growth factor (LMW BCGF) proliferative pathway.
- To compare B-cell precursor ALL with normal B-cell differentiation.
Main Methods:
- Incubation of B-cell precursor ALL cells in culture medium.
- Detection of B8.7 antigen expression via immunophenotyping.
- Assessment of LMW BCGF responsiveness.
- Inhibition studies using anti-B8.7 monoclonal antibody.
Main Results:
- B8.7 antigen was expressed in 72% of B-cell precursor ALL cases studied.
- ALL cells showed increased responsiveness to LMW BCGF after incubation.
- A significant correlation was found between B8.7 expression and LMW BCGF responsiveness.
- Anti-B8.7 antibody inhibited LMW BCGF-dependent proliferation in a dose-dependent manner.
Conclusions:
- B8.7 antigen is expressed at early stages of B-cell differentiation in ALL.
- B8.7 antigen appears functionally linked to the LMW BCGF pathway.
- B-cell precursor ALL cells share similarities with normal B-cells in their response to growth factors and immunoregulatory cytokines.
Abstract:
The purpose of this study was to analyze the expression of B8.7 antigen and its implication in the low molecular weight B-Cell growth factor (LMW BCGF) proliferative pathway at the early stages of the human B-cell differentiation. After an overnight incubation in culture medium of B-cell precursor acute lymphoblastic leukemias (ALL), we demonstrated the presence of B8.7 antigen in 18 of 25 cases (72%). Such an incubation also induced a significant increase in the LMW BCGF responsiveness of ALL cells (P less than 0.03). In addition, we showed a significant correlation between B8.7 expression and the ability of pre-B ALL cells to respond to LMW BCGF. As previously described for normal B cells, the anti-B8.7 monoclonal antibody inhibited the LMW BCGF-dependent proliferation of pre-B ALL cells in a dose-dependent manner. These data indicate that B8.7 antigen is expressed and may be functionally related to the LMW BCGF pathway at the pre-B cell stages of differentiation. These results also suggest that human B-cell precursor ALL are not only phenotypically similar to their normal B lymphocyte counterparts, but are also sensitive to the same immunoregulatory cytokines that control normal cell growth.
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